Variant (rsID / SNP)
rs2032349
rs2032349 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ADH4. Location: chromosome 4, position 100,062,819. The table records no clinical significance for this variant.
Reference-table entries
ADH4Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 4:100062819
- HGVS
- NM_001306171.2,c.192T>C,p.Ser64Ser
- Allele change
- Silent
Associated conditions / phenotypes
Fabry Disease
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.